Canonical Allele Identifier: CA2629370567
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323446del , CM000677.2:g.73323446del GRCh38
NC_000015.9:g.73615787del , CM000677.1:g.73615787del GRCh37
NC_000015.8:g.71402840del NCBI36
NG_009063.1:g.50824del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2652del MANE Select ENSP00000261917.3:p.Ala886ProfsTer14
ENST00000261917.3:c.2652del ENSP00000261917.3:p.Ala886ProfsTer14
NM_005477.2:c.2652del NP_005468.1:p.Ala886ProfsTer14
XM_011521148.1:c.1434del XP_011519450.1:p.Ala480ProfsTer14
XM_011521148.2:c.1434del XP_011519450.1:p.Ala480ProfsTer14
NM_005477.3:c.2652del MANE Select NP_005468.1:p.Ala886ProfsTer14